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Ear, nose and throat Respiratory

Sore throat - acute

Last revised in May 2026

The term 'sore throat' describes the symptom of pain at the back of the mouth.

Sore throat - acute: Summary

  • The term 'sore throat' describes the symptom of pain at the back of the mouth. Clinical descriptions of acute sore throat include:
    • Acute pharyngitis: inflammation of the part of the throat behind the soft palate (oropharynx).
    • Tonsillitis: inflammation of the tonsils.
  • Acute sore throat is usually caused by a viral or bacterial infection. Non-infectious causes are uncommon and include physical irritation from gastro-oesophageal reflux disease or chronic cigarette smoke, and hayfever.
  • Common causes of sore throat in primary care are usually not life-threatening and include common cold, influenza, streptococcal infection, and infectious mononucleosis.
  • Less common causes include HIV, gonococcal pharyngitis, and diphtheria.
  • Acute throat infections most commonly occur in people aged 5–24 years.
  • Complications include otitis media (most common), peri-tonsillar abscess (quinsy), and parapharyngeal abscess.
  • Sore throat due to a viral or bacterial cause is a self-limiting condition. Symptoms resolve within 3 days in 40% of people, and within 1 week in 85% of people, irrespective of whether or not the sore throat is due to a streptococcal infection.
  • The symptoms of infectious mononucleosis usually resolve within 1–2 weeks although mild cases may resolve within days. However, lethargy continues for some time afterwards and in rare cases may continue for months or years.
  • Management of a person presenting with a sore throat involves:
    • Admitting the person immediately if they have stridor, breathing difficulty, clinical dehydration, or a condition that is immediately life-threatening such as acute epiglottis or Kawasaki disease.
    • Referring people with a suspected serious but not immediately life-threatening cause for sore throat (such as cancer or HIV).
    • Giving simple advice, if appropriate, for example, regular use of paracetamol or ibuprofen to relieve pain and fever, and adequate fluid intake to avoid dehydration until the discomfort and swelling subside.
    • Prescribing antibiotic treatment, if appropriate. FeverPAIN and Centor clinical prediction scores should be used to assist the decision on whether to prescribe an antibiotic.
    • Arranging specialist assessment for people with recurrent tonsillitis (a frequency of more than 7 episodes per year for one year, 5 per year for 2 years, or 3 per year for 3 years) as they may benefit from tonsillectomy.

Have I got the right topic?

From birth onwards.

This CKS topic covers the management of acute sore throat due to pharyngitis or tonsillitis.

This CKS topic does not cover the management of chronic sore throat, hoarseness or laryngitis.

There are separate CKS topics on Common cold, Glandular fever (infectious mononucleosis), and Sinusitis.

The target audience for this CKS topic is healthcare professionals working within the NHS in the UK, and providing first contact or primary healthcare.

How up-to-date is this topic?

Changes

May 2026 — minor update. Dosing for phenoxymethylpenicillin amended.

Previous changes

September 2024 — minor update. Drug interactions for phenoxymethylpenicillin updated and aligned with the prescribing section of sinusitis.

May 2024 — minor update. Information added stating that concomitant treatment with clarithromycin and ivabradine is now contra-indicated and caution is now advised when co-administering clarithromycin with edoxaban, as per the manufacturer's updated SPC.

December 2023 — minor update. Update to drug interactions section for erythromycin to include information on interactions with Lomitapide and Corticosteroids, as per the manufacturer's Summary of Product Characteristics (SPC).

August 2023 — minor update. Clarification on the use of rapid antigen testing in sore throat added. NICE do not recommend this test and instead advise the use of clinical risk scoring. 

July 2023 — minor update. The summary of manufacturer’s product characteristics for clarithromycin was updated to include a warning regarding concomitant treatment with domperidone (due to the risk of QT prolongation and cardiac arrhythmias).

February 2023 — reviewed. A literature search was conducted in December 2022 to identify evidence-based guidelines, UK policy, systematic reviews, and key RCTs published since the last revision of the topic. Recommendations were updated to align with the updated NICE guideline Sore throat (acute): antimicrobial prescribing.

December 2022 — minor update. Antibiotic recommendations updated in line with the UKHSA Group A streptococcus in children. Interim clinical guidance summary issued on December 16.  Antibiotic recommendations updated in line with the UKHSA Group A streptococcus in children. Interim clinical guidance summary issued on December 9. 

January 2021 — minor update. Contraindications and drug interactions for erythromycin have been updated in line with an MHRA drug safety update. 

June 2018 — minor update. Removal of the recommendation to use anaesthetic spray to provide temporary pain relief. 

January 2018 — minor update. Incorporated updates from NICE NG 84 Short guideline Sore throat (acute): antimicrobial prescribing. This includes the FeverPAIN and Centor criteria. 

June to August 2017 — reviewed. A literature search was conducted in June 2017 to identify evidence-based guidelines, UK policy, systematic reviews, and key randomized controlled trials published since the last revision of this topic. The topic has undergone restructuring. No major changes to the recommendations have been made.

July 2015 — minor update. The prescribing information sections on erythromycin and clarithromycin have been clarified.

February 2014 — minor update. Text in prescribing information has been changed to state that additional contraceptive precautions are not required during or after courses of clarithromycin.

February 2013 — minor update. The 2013 QIPP options for local implementation have been added to this topic.

October 2012 — reviewed. A literature search was conducted in September 2012 to identify evidence-based guidelines, UK policy, systematic reviews, and key RCTs published since the last revision of the topic. Changes were made to emphasis the use of tonsillectomy selection criteria and the Centor clinical prediction score in recommendations.

July 2011 — minor update. More precise paracetamol dosing for children has been introduced by the Medicines and Healthcare products Regulatory Agency. Prescriptions have been updated to reflect the revised dosing. 

June 2011 — minor update. The 2010/2011 QIPP options for local implementation have been added to this topic. 

April 2011 — topic structure revised to ensure consistency across CKS topics — no changes to clinical recommendations have been made.

February 2011 — minor update. The length of course of treatment for people requiring treatment with a macrolide (because of penicillin allergy) has been amended to 5 days. 

September 2010 — minor update. The Centor criteria have been added. 

February 2010 — minor update. The text regarding investigations for suspected glandular fever (infectious mononucleosis) has been updated. 

August 2009 — minor update. The text regarding when to prescribe an antibiotic and been made clearer. 

March 2009 — minor update. Advice about delayed antibiotic prescribing updated in line with NICE guidance on Respiratory tract infections — antibiotic prescribing. Prescribing of antibiotics for self-limiting respiratory tract infections in adults and children in primary care, and minor changes to the text in the Supporting Evidence section on antibiotic treatment. Issued in April 2009.

January to April 2008 — converted from CKS guidance to CKS topic structure. The evidence-base has been reviewed in detail, and recommendations are more clearly justified and transparently linked to the supporting evidence. There are no major changes to the recommendations.

December 2008 — minor update. Clarithromycin added as an alternative antibiotic to erythromycin, for people who are allergic to penicillin. 

October 2006 — minor update. Analgesia prescriptions updated because new doses of ibuprofen for children are recommend by the British National Formulary.

November 2005 — minor technical update. 

May 2004 — reviewed. Validated in September 2004 and issued in November 2004.

April 2002 — updated to incorporate referral advice from the National Institute for Health and Care Excellence. 

January 2001 — reviewed. Validated in July 2001 and issued in October 2001.

September 1998 — written, replacing guidance on Acute pharyngitis, Acute laryngitis, Acute tonsillitis and Streptococcal sore throat.

Update

New evidence

Evidence-based guidelines

No new evidence-based guidelines since 1 January 2023.

HTAs (Health Technology Assessments)

No new HTAs since 1 January 2023.

Economic appraisals

No new economic appraisals relevant to England since 1 January 2023.

Systematic reviews and meta-analyses

Primary evidence

Otitis media - acute

New policies

No new national policies or guidelines since 1 January 2023.

New safety alerts

No new safety alerts since 1 January 2023.

Changes in product availability

No changes in product availability since 1 January 2023.

Goals and outcome measures

Goals

To support primary healthcare professionals to:

  • Make a diagnosis of the likely cause of a sore throat.
  • Offer advice on alleviation of symptoms.
  • Prescribe treatment where appropriate.
  • Refer to secondary care if necessary.

Outcome measures

No outcome measures were found during the review of this topic.

Audit criteria

No audit criteria were found during the review of this topic.

QOF indicators

No QOF indicators were found during the review of this topic.

QIPP - options for local implementation

No QIPP indicators were found during the review of this topic.

NICE quality standards

No NICE quality standards were found during the review of this topic.

Background information

What is it?

  • Sore throat occurs when an acute upper respiratory tract infection affects the mucosa of the throat.
  • Clinical descriptions of acute sore throat include:
    • Acute pharyngitis: inflammation of the part of the throat behind the soft palate (oropharynx).
    • Tonsillitis: inflammation of the tonsils. May occur in isolation or as part of a generalised pharyngitis.

[Kenealy, 2014; BMJ Best Practice, 2023a; BMJ Best Practice, 2023b]

What causes it?

  • Acute sore throat is most commonly due to viral organisms [BMJ Best Practice, 2023a].
  • Common infectious causes of acute sore throat include [Kenealy, 2014; BMJ Best Practice, 2023a]:
    • Rhinovirus, coronavirus, parainfluenza virus.
    • Influenza types A and B.
    • Streptococcal infection.
      • Group A beta-haemolytic streptococcus (GABHS), also known as Streptococcus pyogenes, is the most common bacterial cause of sore throat and may cause pharyngitis, tonsillitis, or scarlet fever.
      • Group C and G beta-haemolytic streptococci may cause pharyngitis and tonsillitis and have been associated with food-borne outbreaks of pharyngitis.
    • Adenovirus, leading to pharyngoconjunctival fever.
    • Herpes simplex virus type 1 (and more rarely type 2), leading to acute herpetic pharyngitis.
    • Epstein-Barr virus, leading to infectious mononucleosis (glandular fever).
    • Fusobacterium necrophorum, which may cause pharyngitis or tonsillitis, and can (very rarely) lead to Lemierre syndrome (septic phlebitis of the internal jugular vein). 
  • Rarer infectious causes include [Kenealy, 2014; BMJ Best Practice, 2023a]:
    • Haemophilus influenza type b — can cause epiglottitis.
    • Enteroviruses — can cause herpangina and hand, foot, and mouth disease.
    • Measles virus.
    • Candida albicans — causes candidal pharyngitis. May be more common in immunocompromised people, including those undergoing chemotherapy and/or oropharyngeal irradiation.
    • Neisseria gonorrhoeae — can cause gonococcal pharyngitis.
    • Corynebacterium diphtheria, C. ulcerans — cause diphtheria.
    • Arcanobacterium haemolyticum — causes arcanobacterial pharyngitis.
    • Yersinia enterocolitica — causes yersinial pharyngitis.
    • Francisella tularensis — causes oropharyngeal tularaemia.
    • Chlamydophila pneumoniae, Mycoplasma pneumonia — can cause chlamydial pharyngitis and mycoplasmal pharyngitis.
    • HIV-1.
  • Non-infectious causes are uncommon, and include [Kenealy, 2014]:
    • Physical irritation (e.g. from a nasogastric tube or from smoke).
    • Hayfever.
    • Gastro-oesophageal reflux disease.
    • Kawasaki disease — usually presents with fever and the diagnosis is established on the presence of clinical criteria. Throat symptoms may occur.
    • Oral mucositis secondary to radiotherapy or chemotherapy, which may become secondarily infected.
    • Haematological disorders [Viani and Donnelly, 1998]:
      • Leukaemia: ulceration and haemorrhage of the mucous membrane of the pharynx may occur.
      • Aplastic anaemia: sloughing and ulceration of the mouth and pharynx may occur.
    • Drugs which can cause blood disorders (e.g. neutropenia, agranulocytosis, thrombocytopenia) leading to infection and acute sore throat. These include cytotoxic drugs, carbimazole, clozapine, and sulfasalazine  [BNF, 2023].

How common is it?

  • Sore throat is a common condition. In a survey study conducted in Scotland, 31% of adults reported a severe sore throat in the previous year, with 38% of these people visiting a doctor [Kenealy, 2014].
  • It is estimated that an average-sized UK general practice, with a list size of 7,000 patients, will have around 550 consultations for sore throat each year [Guillford, 2016].
  • The highest incidence is in children during the winter months [BMJ Best Practice, 2023a].
  • Recurrent sore throat has an incidence in general practice in the UK of 100 per 1,000 population per year [Georgalas et al, 2014].
  • Bacterial pharyngitis is more common in winter (or early spring), while enteroviral infection is more common in the summer and autumn [BMJ Best Practice, 2023a].
  • Colonisation with group A Streptococcus (leading to pharyngitis) reaches its peak in school-aged children (up to 20%) during the winter months. However, group A Streptococcus infection typically accounts for less than one third of all cases of acute pharyngitis [BMJ Best Practice, 2023a].

What are the complications?

  • Complications of streptococcal pharyngitis/tonsillitis are rare.
    • Scarlet fever is simply the presence of a characteristic 'scarlatina' rash due to infection with an erythrogenic toxin-producing strain of streptococci (usually group A but also can be type B or C).
    • Suppurative complications include:
      • Otitis media (most common).
      • Acute sinusitis — rare, occurring in approximately 0.4% of untreated cases within 2 weeks of an acute tonsilitis.
      • Peri-tonsillar abscess (quinsy) — occurs in approximately 2% of cases within 2 months of an acute tonsilitis, and can pose a risk of airway compromise, aspiration of pus, and death due to vascular involvement. 
    • Non-suppurative complications include acute rheumatic fever, acute glomerulonephritis and reactive arthritis, although these are rare in developed countries.
  • Pharyngitis/tonsillitis as a result of Fusobacterium necrophorum infection can (very rarely) lead to Lemierre disease (sepsis and jugular vein thrombosis). 

[Georgalas et al, 2014; Kenealy, 2014; BMJ Best Practice, 2023a; BMJ Best Practice, 2023b]

What is the prognosis?

  • Sore throat due to a viral or bacterial cause is a self-limiting condition which generally resolves within two weeks [Georgalas et al, 2014; Kenealy, 2014; BMJ Best Practice, 2023a]:
    • A sore throat will spontaneously resolve by 3 days in about 40% of people.
    • By 1 week, approximately 85% of people are symptom-free. 
  • The symptoms of infectious mononucleosis usually resolve within 1–2 weeks although mild cases may resolve within days. However lethargy continues for some time afterwards and in rare cases may continue for months or years [Rezk, 2015; De Paor, 2016].

Diagnosis of sore throat

How do I diagnose the cause of a sore throat?

Note: There is no evidence that sore throats caused by bacterial infection are more severe than those caused by viral infection, or that the duration of the illness is significantly different in either case. The precise diagnosis may be clinically significant in more severe cases or of epidemiological interest. 

To identify the underlying cause of a sore throat:

  • Examine the person's throat and neck:
    • Pharyngitis is often associated with pharyngeal exudate and cervical lymphadenopathy.
    • Tonsillitis is associated with tonsillar exudate with enlargement and erythema of the tonsils. There may be anterior cervical lymphadenopathy.
  • Ask the person about their symptoms. Non-specific symptoms may include:
    • Headache, nausea, vomiting, and abdominal pain — may be present in children with pharyngitis, and all people with tonsillitis.
    • Fever — this is common in pharyngitis and tonsillitis. Most people with acute tonsillitis have a fever over 38°C.
    • Note: Rhinorrhoea, nasal congestion, and cough are usually present in viral pharyngitis, but not in bacterial pharyngitis.
  • Be aware that a sore throat may occasionally result in significantly reduced fluid intake, which may lead to dehydration.
    • Ask the person about recent fluid intake if pain on swallowing is significant.
    • For babies and young children, ask the parent/carer about the number of wet nappies, whether fluid intake is significantly reduced (50-75% normal volume) and examine the child for signs of clinical dehydration (reduced skin turgor and/or a capillary refill time of more than three seconds, and/or dry mucous membranes).
  • Consider the person's signs and symptoms, and use the FeverPAIN or Centor clinical prediction score to determine the likelihood of streptococcal infection (and therefore the need for antibiotic treatment):
    • Acute Group A streptococcal (GAS) pharyngitis/tonsillitis is common in children and adolescents aged 5 to 15 years and is more common in the winter (or early spring) in temperate climates.  Streptococcal infection is suggested by fever over 38.5°C, exudate on the pharynx/tonsils, anterior neck lymphadenopathy, and absence of cough. A scarlatiniform rash may be present, especially in children. For more information, see the CKS topic on Scarlet fever.
    • The FeverPAIN criteria: score 1 point for each (maximum score of 5).
      • Fever (during previous 24 hours). 
      • Purulence (pharyngeal/tonsillar exudate).
      • Attend rapidly (within 3 days after onset of symptoms).
      • Severely Inflamed tonsils.
      • No cough or coryza.
    • A score of 0 or 1 is associated with a 13-18% likelihood of isolating streptococcus. A score of 2 or 3 is associated with a 34-40% likelihood of isolating streptococcus. A score of 4 or 5 is associated with a 62-65% likelihood of isolating streptococcus.
    • Centor criteria: score 1 point for each (maximum score of 4).
      • Tonsillar exudate.
      • Tender anterior cervical lymphadenopathy or lymphadenitis.
      • History of fever (over 38°C).
      • Absence of cough.
    • A score of 0, 1 or 2 is thought to be associated with a 3-17% likelihood of isolating streptococcus. A score of 3 or 4 is thought to be associated with a 32-56% likelihood of isolating streptococcus.
    • NICE do not recommend the use of rapid antigen testing. 
  • Other common (non-streptococcal) infectious causes of acute sore throat, and their signs and symptoms include:
    • The common cold — suggested by rhinorrhoea, nasal congestion, and cough.  For more information, see the CKS topic on the Common cold.
    • Influenza — suggested by headache, weakness and fatigue, myalgia, malaise, anorexia, insomnia, a dry, unproductive cough, and fever. For more information, see the CKS topic on Influenza - seasonal.
    • Pharyngoconjunctival fever — suggested by fever and conjunctivitis. Malaise, myalgia, headache, rhinitis and cervical adenitis may also be present.
    • Acute herpetic pharyngitis — suggested by vesicles and shallow ulcers on the palate (although these are not always present). There may be cervical lymphadenopathy, fever, and exudate. If there is an associated gingivostomatitis, vesicles and ulcers are also present on the labial and buccal mucosa. For more information, see the CKS topic on Herpes simplex - oral.
    • Infectious mononucleosis (glandular fever) — suggested by pharyngitis of longer than several days' duration, adenopathy, and splenomegaly. A serum monospot test should be carried out to confirm the diagnosis (in people over 4 years of age) and full blood count should also be considered — a raised WBC count with lymphocytosis and atypical lymphocytes is suggestive of infectious mononucleosis. For more information, see the CKS topic on Glandular fever (infectious mononucleosis).
    • COVID-19 — suggested by fever, a new continuous cough, shortness of breath, malaise, muscle aches and pains, rhinorrhoea and gastrointestinal symptoms. For more information, see the CKS topic on Coronavirus - COVID-19.
  • Rarer infectious causes of sore throat include:
    • Herpangina — suggested by acute onset of fever, sore throat, and dysphagia, and also vomiting and abdominal symptoms. Small vesicles (1–2 mm) may be seen on the soft palate, fauces, palate, uvula, and tonsils, which rupture to become small white ulcers. The condition usually affects people of 2–20 years of age and most commonly occurs in the late summer and autumn.
    • Hand, foot, and mouth disease — suggested by fever (typically 38–39°C), malaise, loss of appetite, cough, abdominal pain, and sore mouth that precede the development of tender lesions in the mouth and/or vesicles on the palms of the hands and soles of the feet. Children younger than 4 years of age are most commonly affected and it most commonly occurs in the late summer and autumn. For more information, see the CKS topic on Hand foot and mouth disease.
    • HIV-1— sore throat may be a feature of primary HIV infection and occurs after an incubation period of 3–5 weeks, with myalgia, arthralgia, lethargy, and in some people a non-itchy maculopapular rash. Lymphadenopathy develops a week later. For more information, see the CKS topic on HIV infections and AIDS.
    • Gonorrhoea — causes mild pharyngitis which may be accompanied by anterior cervical adenopathy. Should be considered in sexually active or abused individuals with pharyngitis, especially in those with negative cultures for GAS. Take throat swabs for culture to confirm the diagnosis. For more information, see the CKS topic on Gonorrhoea.
    • Diphtheria — consider if oropharyngeal membranes appear grey/green, and/or the person has not been vaccinated. Take throat swabs for culture to confirm the diagnosis. 
    • Measles —  suggested by conjunctivitis, rhinitis, cough, and characteristic maculopapular rash in a person who is non-vaccinated. Koplik spots (bluish-white, raised lesions on an erythematous base on the buccal mucosa) are characteristic. 
    • Arcanobacterial pharyngitis —  suggested by a diffuse, sometimes itchy, erythematous maculopapular rash on the extremities and trunk. Pharyngeal exudate and cervical lymphadenopathy are commonly present.
    • Yersinial pharyngitis — this is associated with contaminated food and drink, but in adults may occur without gastrointestinal symptoms. Rarely, there may be a fulminant course with a high mortality rate. Fever, prominent cervical lymphadenopathy, and abdominal pain with or without diarrhoea have been reported.
    • Tularaemia — may be suggested by pharyngeal ulceration and exudate, and a history of ingestion of undercooked wild animal meat. The pharyngitis may have previously failed to respond to penicillin. Take throat swabs for culture to confirm the diagnosis. 
    • Chlamydial pharyngitis, mycoplasmal pharyngitis— may occur in association with pneumonia or bronchitis but otherwise have no clear distinguishing features. Chlamydial pharyngitis should be considered in sexually active or abused individuals with pharyngitis, especially in those with negative cultures for GAS. Take throat swabs for culture to confirm the diagnosis. For more information, see the CKS topic on Chlamydia - uncomplicated genital.
    • Candida albicans — may cause pharyngitis in immunosuppressed individuals, people who use inhaled corticosteroids, or those undergoing chemotherapy or irradiation for oropharyngeal cancer.
    • Retropharyngeal or peritonsillar abscess — may present with sore throat, fever, neck pain and muffled voice, and is most common in children 2 to 4 years old, or older children with a history of oral or pharyngeal trauma.
  • Non-infectious causes include:
    • Physical irritation — consider in people with a nasogastric tube, or who smoke.
    • Hayfever. For more information, see the CKS topic on Allergic rhinitis.
    • Gastro-oesophageal reflux disease. For more information, see the CKS topic on Dyspepsia - proven GORD.
    • Kawasaki disease — may occasionally present as sore throat without exudate. The cause of Kawasaki disease is unknown. The majority of cases occur in children under 4 years of age. Kawasaki disease is diagnosed by the presence of either five of the six main symptoms, or four main symptoms if coronary aneurysms are identified by echocardiography. The six main symptoms are:
      • Fever of unknown aetiology lasting 5 days or more.
      • Bilateral conjunctivitis.
      • Changes in the lips and oral cavity (dryness and fissuring of the lips, and redness of the oral cavity and pharynx).
      • Cervical lymphadenopathy.
      • Polymorphous rash (a combination of morbilliform, scarlatiniform, urticariform, or erythema multiforme-like rash).
      • Changes in the extremities (reddening of the palms and soles, desquamation of the skin, and oedema of the hands and feet).
    • Oral mucositis secondary to radiotherapy or chemotherapy, which may become secondarily infected. For more information see the CKS topic on Palliative care - oral.
    • Haematological disorders: 
      • Leukaemia: ulceration and haemorrhage of the mucous membrane of the pharynx may occur. For more information, see the CKS topic on Haematological cancers - recognition and referral.
      • Aplastic anaemia: sloughing and ulceration of the mouth and pharynx may occur.
    • Drugs that can cause blood disorders (e.g. neutropenia, agranulocytosis, thrombocytopenia) leading to infection and acute sore throat. These include cytotoxic drugs, carbimazole, clozapine, and sulfasalazine.
    • Oropharyngeal cancer — suggested by hoarseness, dysphonia, sore throat, difficulty swallowing, and neck mass or adenopathy.
    • Behcet's syndrome — suggested by vesicles on pharynx, genital ulcers, skin and eye lesions.
    • Steven's Johnson syndrome — suggested by vesicles on pharynx, along with more pronounced mucosal changes in a person with recent infections, seizures, or new medications.
  • Be alert for serious underlying causes/complications that can be associated with sore throat, including:
    • Epiglottitis — suggested by severe and acute onset of sore throat and fever, muffled voice, drooling, and stridor.
      • A child with epiglottitis prefers to sit leaning forward. Breathing tends to be tentative and careful, without marked increase in respiration rate. Inspiratory stridor and hoarseness may occur. Tachycardia may be out of proportion to the fever if hypoxia is present.
      • In adults, predictors of airway compromise include sitting erect, stridor, and dyspnoea.
      • Note: Do not examine the throat of anyone with suspected epiglottitis as this may precipitate closure of the airway.
    • Peritonsillar abscess (quinsy) — suggested by fever, neck pain, trismus, a muffled voice, a displaced uvula, and an enlarged, displaced tonsil, with swelling of the peri-tonsillar region. It is most common in children 2 to 4 years of age.
    • Retropharyngeal abscess — suggested by severe sore throat that does not resolve after a few days. There may be trismus or visible neck swelling.
    • Lemierre syndrome — thrombophlebitis of the jugular vein. Typically seen in people with systemic inflammatory response syndrome (SIRS) or sepsis.

Basis for recommendation

Information on diagnosing the cause of acute sore throat is based on expert opinion in BMJ Best Practice clinical guidelines on Acute Pharyngitis [BMJ Best Practice, 2023a] and Tonsillitis [BMJ Best Practice, 2023b], narrative review articles published in BMJ Clinical Evidence [Kenealy, 2014]; [Georgalas et al, 2014], a German clinical practice guideline Sore Throat [Krüger, 2021], NICE guidance Sore throat (acute): antimicrobial prescribing [NICE, 2023], and Cochrane systematic reviews [Cohen, 2016; Cohen, 2020].

Some authors advise the use of rapid antigen testing in suspected GAS, particularly where the diagnosis of GAS needs to be confirmed with certainty (such as in people at high risk of rheumatic fever, vulnerable people such as the very old or young, or people who are at risk of immunosuppression, or people with very severe symptoms). However, NICE advise the use of clinical risk scoring on the grounds of clinical effectiveness in affecting outcomes and microbial stewardship [NICE, 2023; BMJ Best Practice, 2023a]. 

Management

Scenario: Management

From birth onwards.

How should I manage a sore throat in primary care?

  • Arrange 999 ambulance transfer for anyone with suspected epiglottitis, so that the epiglottis can be examined where there is capacity to carry out immediate intubation should the airway close. 
  • Arrange hospital admission, with urgency determined by clinical judgement, for anyone with:
    • Breathing difficulty.
    • Clinical dehydration.
    • Peri-tonsillar abscess or cellulitis, parapharyngeal abscess, retropharyngeal abscess, or Lemierre syndrome (as there is a risk of airway compromise or rupture of the abscess).
    • Signs of marked systemic illness or sepsis. 
    • A suspected rare cause such as Kawasaki disease, diphtheria, tularaemia, or yersinial pharyngitis.
      • Use clinical judgement to determine whether hospital admission is necessary in vulnerable people (e.g. infants, very old people, those who are immunosuppressed or immunocompromised), as pharyngitis/tonsillitis may run a more severe course.
  • If the person is taking a disease-modifying anti-rheumatic drug (DMARD) and immediate admission is not appropriate:
    • Take blood for a full blood count (FBC). Arrange to contact them later with the result.
    • Withhold the DMARD whilst awaiting the result and until discussed with the hospital rheumatology service (or follow local protocols).
    • Seek urgent specialist advice/referral if the person has a low white cell count or deteriorates.
    • Consider prescribing an antibiotic.
  • If the person is taking carbimazole (which can cause idiosyncratic neutropenia):
    • Take an urgent FBC and withhold the drug until the result is available.
    • Seek specialist advice.
    • Consider prescribing an antibiotic.
  • If the person is on chemotherapy, has known or suspected leukaemia, asplenia, aplastic anaemia or HIV/AIDS, or is taking an immunosuppressive drug following a transplant:
    • Seek immediate specialist advice or referral.
    • Meanwhile check the FBC urgently.
  • Refer or seek urgent specialist advice for anyone who has severe oral mucositis. For further information, see the CKS topic on palliative care - oral.
  • Arrange appropriate specialist referral for anyone with a suspected serious (but not immediately life-threatening) cause for sore throat (such as cancer or HIV), with urgency determined by clinical judgement.
  • Offer an immediate antibiotic prescription to people who are systemically very unwell, have symptoms and signs of a more serious illness or condition, or are at high-risk of complications.
  • For people with:
    • A FeverPAIN score of 4 or 5, or Centor criteria score of 3 or 4 (or if group A streptococcus [GAS] has been confirmed by rapid antigen testing) — consider an immediate antibiotic prescription or a back-up antibiotic prescription, taking into account:
      • The unlikely event of complications if antibiotics are withheld.
      • Possible adverse effects, particularly of diarrhoea and nausea.   
    • A FeverPAIN score of 2 or 3 — consider no antibiotic prescription, or a back-up antibiotic prescription, taking into account:
      • Evidence that antibiotics make little difference to how long symptoms last (on average, they shorten symptoms by about 16 hours).
      • Evidence that most people feel better after 1 week, with or without antibiotics.
      • The unlikely event of complications if antibiotics are withheld.
      • Possible adverse effects, particularly diarrhoea and nausea.
    • A FeverPAIN score of 0 or 1, or Centor score of 0,1, or 2 — do not offer an antibiotic prescription.
      • Advise that an antibiotic is not needed, and that they should seek medical help if symptoms worsen rapidly or significantly, do not start to improve after 1 week, or they become systemically very unwell.  
  • If a back-up antibiotic prescription is given, advise the person that:
    • An antibiotic is not needed immediately.
    • The back-up antibiotic should be used if symptoms do not start to improve within 3 to 5 days, or if they worsen rapidly or significantly at any time.
  • Prescribe phenoxymethylpenicillin first-line.
    • For people with penicillin allergy, prescribe clarithromycin. 
    • Prescribe erythromycin for a pregnant woman with penicillin allergy.
    • For information on dosing, contraindications and cautions, adverse effects, and drug interactions, see the section on Prescribing information.
  • If gonococcal or chlamydial infection is confirmed, treat appropriately. For more information, see the CKS topics on Gonorrhoea and Chlamydia - uncomplicated genital.
  • If infectious mononucleosis is confirmed, see the CKS topic on Glandular fever (infectious mononucleosis) for advice on management.
  • If candidal pharyngitis is suspected, prescribe nystatin for mild to moderate cases, and fluconazole if the fungal infection is more widespread or the person has experienced a long duration of symptoms. For more information, including prescribing information, see the CKS topic on Candida - oral.
  • Advise all people with acute sore throat that:
    • Symptoms may last for around 1 week.
    • They should seek medical help if symptoms worsen rapidly or significantly, or they become very unwell.
    • Adequate fluid should be taken during the course of the illness.
    • Ibuprofen and paracetamol can be used as an antipyretic and/or analgesic.
    • Medicated lozenges (containing a local anaesthetic, a nonsteroidal anti-inflammatory drug [NSAID] or an antiseptic) may provide temporary relief from throat pain.
    • Hot drinks should be avoided as these can exacerbate pain.
    • Children may return to school or day care after fever has resolved and they are no longer feeling unwell, and/or after taking antibiotics for at least 24 hours.
  • Routine follow-up is not required, however, the person should be advised to seek follow-up if:
    • Symptoms have not improved after 3 or 4 days of antibiotic therapy — so that alternative diagnoses can be considered.
    • Pain does not improve after 3 days, and/or there is fever over 38.3°C — so that antibiotic treatment can be initiated (if not in place already) or alternative diagnoses can be considered.
    • It becomes difficult to swallow saliva or liquids, if any difficulty in breathing develops, or if there is any one-sided neck or throat swelling — so that the need for hospital admission can be reassessed (the person should be advised to seek advice urgently in these scenarios).
  • For people with severe recurrent tonsillitis (a frequency of more than 7 episodes per year for one year, 5 per year for 2 years, or 3 per year for 3 years, and for whom there is no other explanation for the recurrent symptoms), referral to an ear, nose, and throat specialist is advised as this cohort may benefit from tonsillectomy.

Basis for recommendation

The recommendations are largely based on expert opinion in the BMJ Best Practice guidelines Acute Pharyngitis [BMJ Best Practice, 2023a], and Tonsillitis [BMJ Best Practice, 2023b], a National Heart Foundation of New Zealand guideline Group A Streptococcal Sore Throat Management [National Heart Foundation of New Zealand, 2019], a German clinical practice guideline Sore Throat [Krüger, 2021], Cochrane systematic reviews [van Driel, 2016; de Cassan, 2020; Spinks, 2021; Spurling, 2017], and the National Institute for Health and Care Excellence (NICE) guideline Sore throat (acute): antimicrobial prescribing [NICE, 2023].

Admission
  • The information on when to admit a person with sore throat is based on the opinions of previous expert reviewers of this CKS topic, and is pragmatic, based on what CKS considers to be good medical practice.
Referral
  • The information on when to refer a person with sore throat is also based on expert opinion within medical textbooks [Jones, 1998], [Franco and Har-El, 1999], [Dhillon and East, 2006; BMJ Best Practice, 2023b], and is pragmatic, based on what CKS considers to be good medical practice.
  • The information on when to refer a person to an ear, nose, and throat specialist is based on expert opinion published in review articles and clinical guidelines:
    • Recurrent tonsillitis is a common indication for otolaryngology consultation. Several studies have demonstrated modest benefit for tonsillectomy in children having recurrent tonsillitis [Randall, 2020].
    • The American Academy of Otolaryngology–Head and Neck Surgery guidelines (AAOHNS guidelines) advise that children with 7 bouts of tonsillitis in 1 year, 5 annual bouts for 2 years, or 3 annual bouts for 3 years may benefit from tonsillectomy [Mitchell, 2019].
    • Tonsillectomy can reduce the number of days and episodes of sore throat in the first year, with more benefit in children who were more severely affected, and is associated with significant improvements in quality of life [BMJ Best Practice, 2023b].
Follow-up
  • The advice on when a person should seek follow-up is pragmatic, based on what CKS considers to be good medical practice.

Prescribing information

Important aspects of prescribing information relevant to primary healthcare are covered in this section specifically for the drugs recommended in this CKS topic. For further information on contraindications, cautions, drug interactions, and adverse effects, see the electronic Medicines Compendium (eMC), or the British National Formulary (BNF).

Paracetamol and ibuprofen

For detailed prescribing information on paracetamol and ibuprofen, see the CKS topics on Analgesia - mild-to-moderate pain and NSAIDs - prescribing issues.

Clarithromycin and erythromycin

Dose

Clarithromycin

  • In adults, prescribe 250 to 500 mg twice daily for 5 days.
  • In children aged 1 month to 11 years weighing:
    • Up to 8 kg, prescribe 7.5 mg/kg twice daily for 5 days.
    • 8-11 kg, prescribe 62.5 mg twice daily for 5 days.
    • 12-19 kg, prescribe 125 mg twice daily for 5 days.
    • 20-29 kg, prescribe 187.5 mg twice daily for 5 days.
    • 30-40 kg, prescribe 250 mg twice daily for 5 days.
  • In children aged 12-17 years, prescribe 250-500 mg twice daily for 5 days. 

[BNF, 2023; BNFC, 2023; NICE, 2023]

Erythromycin

  • For women who are pregnant, prescribe 250 mg to 500 mg four times daily or 500 mg to 1,000 mg twice daily for 5 days. 

[PHE, 2017; BNF, 2023; NICE, 2023]

Contraindications and cautions

  •  Do not prescribe clarithromycin or erythromycin to people at risk of QT prolongation, including people:
    • Taking drugs that prolong the QT interval (for example haloperidol, sotalol, terfenadine, and pimozide).
    • With hypokalaemia — due to the risk of prolongation of the QT interval.
    • With a history of QT prolongation or ventricular cardiac arrhythmia, including Torsades de pointes.
      • Macrolides can prolong the QT interval.
  • Do not prescribe clarithromycin to people with severe hepatic impairment in combination with renal impairment.
  • Do not prescribe erythromycin to people with porphyria. 
  • Prescribe clarithromycin and erythromycin with caution to people with:
    • Myasthenia gravis — macrolides may aggravate weakness symptoms.
    • Mild to moderate hepatic impairment (or people concomitantly receiving potentially hepatotoxic drugs) — clarithromycin and erythromycin are mainly excreted by the liver.
      • Use half the normal dose of clarithromycin if creatinine clearance is less than 30 mL/min, and for a maximum duration of 14 days. Avoid modified-release preparations in people with creatinine clearance of less than 30 mL/min, and use half the normal dose if creatinine clearance is 30-60 mL/minute.
    • Coronary artery disease, severe cardiac insufficiency, or bradycardia (less than 50 beats per minute) — due to increased risk of QT prolongation.
  • Prescribe erythromycin with caution to people with moderate to severe renal impairment.
    • Give a maximum dose for erythromycin of 1.5 g a day in severe renal impairment due to the risk of ototoxicity.

[ABPI, 2022; EMC, 2023; BNF, 2023]  

Adverse effects

  • Nausea, vomiting, abdominal discomfort, and diarrhoea are the most common adverse effects of macrolides.
    • Consider pseudomembranous colitis if a person develops severe diarrhoea during or after treatment with clarithromycin or erythromycin. Pseudomembranous colitis is an acute, exudative colitis caused by Clostridium difficile, a Gram-positive toxin-releasing bacillus. It often follows antibiotic treatment. For more information, see the CKS topic on Diarrhoea - antibiotic associated.
  • Anaphylaxis is rarely associated with clarithromycin or erythromycin.
  • Hepatotoxicity (including cholestatic jaundice) and rash have been reported following treatment with clarithromycin or erythromycin.
  • Reversible hearing loss (sometimes with tinnitus) can occur after large doses of clarithromycin (1–2 g) or erythromycin (more than 4 g).
  • Other adverse effects reported rarely or very rarely include pancreatitis, QT interval prolongation, arrhythmias, Stevens-Johnson syndrome, and toxic epidermal necrolysis.

[ABPI, 2022; EMC, 2023; BNF, 2023]

Drug interactions

Drug interactions with clarithromycin and erythromycin include:

  • Carbamazepine — clarithromycin and erythromycin inhibit the cytochrome P450 enzyme CYP3A4, resulting in reduced carbamazepine metabolism.
    • Reduce the dose of carbamazepine by 30–50% during treatment with clarithromycin or erythromycin.
    • Advise the person to report symptoms of carbamazepine toxicity (such as dizziness, diplopia, ataxia, or confusion).
  • Corticosteroids — levels of corticosteroids may be increased. Monitor for corticosteroid adverse effects (such as moon face, weight gain, and hyperglycaemia), and adjust the corticosteroid dose or stop the macrolide as appropriate. 
  • Edoxaban — manufacturer advises caution with concurrent treatment with edoxaban, particularly in those with a high risk of bleeding.
  • Ivabradine — concomitant treatment is contra-indicated, owing to CYP3A4 inhibition by clarithromycin which can cause elevated levels of ivabradine.
  • Lomitapide — concurrent use with erythromycin increases transaminase levels and is contraindicated.
  • Rivaroxaban — erythromycin may increase levels of rivaroxaban, increasing the risk of bleeding. 
  • Warfarin — occasionally and unpredictably, the effects of warfarin may be markedly increased by macrolides.
    • Monitor the international normalized ratio (INR), and adjust the warfarin dose accordingly.
  • Statins — there is an increased risk of myopathy (due to cytochrome P450 enzyme CYP3A4 inhibition) if clarithromycin or erythromycin are taken with simvastatin or atorvastatin.
    • For simvastatin —concurrent use with clarithromycin or erythromycin is contraindicated as simvastatin is extensively metabolized by CYP3A4. If treatment with clarithromycin cannot be avoided, stop treatment with simvastatin during the course of treatment.
    • For atorvastatin, avoid concurrent use with clarithromycin or erythromycin, as atorvastatin is moderately metabolised by CYP3A4. If concurrent use cannot be avoided, prescribe the lowest starting dose of atorvastatin (10 mg), and advise the person to report any muscle pain, tenderness, or weakness.
    • Clinically significant drug interactions resulting from cytochrome P450-mediated metabolism are not expected for rosuvastatin and pravastatin as they are not metabolized to a clinically significant extent by the cytochrome P450 system. Fluvastatin is not dependent on CYP3A metabolism; therefore, an interaction with clarithromycin is unlikely. Nevertheless, advise the person to report any muscle pain, tenderness, or weakness.
  • Calcium channel blockers (CCBs) — due to an increased risk of hypotension, caution is advised with the concurrent use of macrolides and CCBs metabolised by CYP3A4 (such as verapamil, amlodipine, and diltiazem).
  • Drugs that prolong the QT interval (such as haloperidol, sotalol, terfenadine, domperidone, and pimozide) — all macrolides can prolong the QT interval, and concomitant use of drugs that prolong the QT interval is not recommended.
    • Seek advice from a microbiologist regarding a suitable alternative antibiotic.
  • Drugs that cause hypokalaemia (such as diuretics, corticosteroids, short-acting beta-2 agonists) — hypokalaemia is a risk factor for QT prolongation.
    • Seek advice from a microbiologist regarding a suitable alternative antibiotic.
  • Theophylline — erythromycin and possibly clarithromycin increase plasma concentrations of theophylline, and theophylline may also reduce absorption of oral erythromycin.
    • Check theophylline levels 48 hours after starting erythromycin, and adjust the dose of theophylline accordingly.

[MHRA, 2020; ABPI, 2022; BNF, 2023; EMC, 2024]

Phenoxymethylpenicillin

Dose

  • In adults, prescribe 500 mg four times daily, or 1000 mg twice daily for 5 to 10 days.
  • In children aged: 
    • 1-11 months, prescribe 62.5 mg 4 times daily, or 125 mg twice daily for 5 to 10 days. 
    • 1-5 years, prescribe 125 mg 4 times daily, or 250 mg twice daily for 5 to 10 days. 
    • 6-11 years, prescribe 250 mg 4 times daily, or 500 mg twice daily for 5 to 10 days. 
    • 12-17 years, prescribe 500 mg 4 times daily, or 1000 mg twice daily for 5 to 10 days. 
  • A 5-day course may be enough for symptomatic cure; but a 10-day course may increase the chance of microbiological cure.

[BNF, 2023; BNFC, 2023; NICE, 2023]

Contraindications and cautions

  • Do not prescribe a penicillin to people with a history of anaphylaxis, urticaria, or rash immediately after penicillin administration due to risk of immediate hypersensitivity.
    • Note: People with a history of a minor rash (i.e. non-confluent, non-pruritic rash restricted to a small area of the body), or a rash that occurs more than 72 hours after penicillin administration are probably not allergic to penicillin and in these individuals, a penicillin should not be withheld unnecessarily for serious infections.
  • Prescribe penicillins with caution to people with a history of atopic allergy (e.g. asthma, eczema, hay fever) as these people are at increased risk of anaphylactic reactions.
  • Phenoxymethylpenicillin should be used cautiously in people with a history of:
    • Cephalosporin-sensitivity, as there is some evidence of partial cross-sensitivity to cephalosporins and penicillins.
    • Antibiotic associated colitis.

[ABPI, 2019; BNF, 2023]

Adverse effects

  • Common adverse effects of penicillins include:
    • Diarrhoea — consider pseudomembranous colitis if a person develops severe diarrhoea during or after treatment with a penicillin. Pseudomembranous colitis is an acute, exudative colitis caused by Clostridium difficile, a Gram-positive toxin-releasing bacillus. It often follows antibiotic treatment. For more information, see the CKS topic on Diarrhoea - antibiotic associated.
    • Fever.
    • Hypersensitivity reactions.
    • Joint pain.
    • Rash.
    • Serum sickness-like reaction.
    • Urticaria.
  • Rare adverse effects include:
    • Anaphylaxis, angioedema.
    • Cerebral irritation.
    • CNS toxicity (including convulsions).
    • Coagulation disorders. 
    • Encephalopathy.
    • Haemolytic anaemia. 
    • Interstitial nephritis. 
    • Leucopenia. 
    • Thrombocytopenia.
    • Neutropenia.

[ABPI, 2019; BNF, 2023]

Drug interactions

  • Drug interactions of phenoxymethylpenicillin include:
    • Methotrexate — reduced clearance and acute methotrexate toxicity have been attributed to concurrent use with some penicillins. Serious interactions are uncommon, but risk factors are as yet unknown. People taking low-dose methotrexate have been affected.
      • High-dose methotrexate: standard routine monitoring will identify any decreases in elimination, which should be managed according to local guidelines.
      • Low-dose methotrexate: consult local or national guidelines for recommendations on appropriate monitoring and management.
    • Warfarin — phenoxymethylpenicillin potentially alters the anticoagulant effect of warfarin.   
      • Monitor the international normalized ratio (INR), and adjust the warfarin dose accordingly.

[EMC, 2019; Preston, 2024; BNF, 2024]

Supporting evidence

This CKS topic is largely based on expert opinions provided in the BMJ Best Practice clinical guidelines on Acute Pharyngitis [BMJ Best Practice, 2023a], Tonsillitis [BMJ Best Practice, 2023b], a National Heart Foundation of New Zealand guideline Group A Streptococcal Sore Throat Management [National Heart Foundation of New Zealand, 2019], a German clinical practice guideline Sore Throat [Krüger, 2021], narrative review articles published in BMJ Clinical Evidence [Kenealy, 2014]; [Georgalas et al, 2014], Cochrane systematic reviews [van Driel, 2016; de Cassan, 2020; Spinks, 2021; Spurling, 2017; Cohen, 2016; Cohen, 2020], and National Institute for Health and Care Excellence (NICE) guideline Sore throat (acute): antimicrobial prescribing [NICE, 2023].

How this topic was developed

This section briefly describes the processes used in developing and updating this topic. Further details on the full process can be found in the About Us section and on the Clarity Informatics website.

Search strategy

A literature search was conducted for guidelines, systematic reviews and randomized controlled trials on primary care management of acute sore throat.

Search dates

July 2017 - January 2023

Key search terms

Various combinations of searches were carried out. The terms listed below are the core search terms that were used for Medline.

  • exp pharyngitis/, exp tonsilitis/, exp pharynx/, exp adenoids/., exp tonsillectomy/, tonsil$.tw., pharyn$.tw., adenoid$.tw., exp acute pain/, (acute ADJ sore throat).tw., pain.tw., sore throat.tw.

Sources of guidelines

Sources of systematic reviews and meta-analyses

  • The Cochrane Library:
    • Systematic reviews
    • Protocols
    • Database of Abstracts of Reviews of Effects
  • Medline (with systematic review filter)
  • EMBASE (with systematic review filter)

Sources of health technology assessments and economic appraisals

Sources of randomized controlled trials

  • The Cochrane Library:
    • Central Register of Controlled Trials
  • Medline (with randomized controlled trial filter)
  • EMBASE (with randomized controlled trial filter)

Sources of evidence based reviews and evidence summaries

Sources of national policy

Patient experiences

Sources of medicines information

The following sources are used by CKS pharmacists and are not necessarily searched by CKS information specialists for all topics. Some of these resources are not freely available and require subscriptions to access content.

Stakeholder engagement

Our policy

The external review process is an essential part of CKS topic development. Consultation with a wide range of stakeholders provides quality assurance of the topic in terms of:

  • Clinical accuracy.
  • Consistency with other providers of clinical knowledge for primary care.
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Principles of the consultation process

  • The process is inclusive and any individual may participate.
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  • Discussion with an individual or an organization about the CKS response to their comments is only undertaken in exceptional circumstances (at the discretion of the Clinical Editor or Editorial Steering Group).
  • All reviewers are thanked and offered a letter acknowledging their contribution for the purposes of appraisal/revalidation.
  • All reviewers are invited to be acknowledged on the website. All reviewers are given the opportunity to feedback about the external review process, enabling improvements to be made where appropriate.

Stakeholders

  • Key stakeholders identified by the CKS team are invited to comment on draft CKS topics. Individuals and organizations can also register an interest to feedback on a specific topic, or topics in a particular clinical area, through the Getting involved section of the Clarity Informatics website.
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Clarity Informatics has enlisted the support and involvement of patients and lay persons at all stages in the process of creating the content which include:

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Our lay and patient involvement includes membership on the editorial steering group, contacting expert patient groups, organizations and individuals.

Evidence exclusion criteria

Our policy

Scoping a literature search, and reviewing the evidence for CKS is a methodical and systematic process that is carried out by the lead clinical author for each topic. Relevant evidence is gathered in order that the clinical author can make fully informed decisions and recommendations. It is important to note that some evidence may be excluded for a variety of reasons. These reasons may be applied across all CKS topics or may be specific to a given topic.

Studies identified during literature searches are reviewed to identify the most appropriate information to author a CKS topic, ensuring any recommendations are based on the best evidence. We use the principles of the GRADE and PICOT approaches to assess the quality of published research. We use the principles of AGREE II to assess the quality of published guidelines.

Standard exclusions for scoping literature:

  • Animal studies
  • Original research is not written in English

Possible exclusions for reviewed literature:

  • Sample size too small or study underpowered
  • Bias evident or promotional literature
  • Population not relevant
  • Intervention/treatment not relevant
  • Outcomes not relevant
  • Outcomes have no clear evidence of clinical effectiveness
  • Setting not relevant
  • Not relevant to UK
  • Incorrect study type
  • Review article
  • Duplicate reference

Organizational, behavioural and financial barriers

Our policy

The CKS literature searches take into consideration the following concepts, which are discussed at the initial scoping of the topic.

  • Feasibility
    • Studies are selected depending on whether the intervention under investigation is available in the NHS and can be practically and safely undertaken in primary care.
  • Organizational and Financial Impact Analysis
  • Studies are selected and evaluated on whether the intervention under investigations may have an impact on local clinical service provision or national impact on cost for the NHS. The principles of clinical budget impact analysis are adhered to, evaluated and recorded by the author. The following factors are considered when making this assessment and analysis.
    • Eligible population
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    • Cost of the current or new intervention mix
    • Impact on other costs
    • Condition-related costs
    • In-direct costs and service impacts
    • Time dependencies
  • Cost-effectiveness or cost-benefit analysis studies are identified where available. 

We also evaluate and include evidence from NICE accredited sources which provide economic evaluations of recommendations, such as NICE guidelines. When a recommended action may not be possible because of resource constraints, this is explicitly indicated to healthcare professionals by the wording of the CKS recommendation.

Declarations of interest

Our policy

Clarity Informatics requests that all those involved in the writing and reviewing of topics, and those involved in the external review process to declare any competing interests. Signed copies are securely held by Clarity Informatics and are available on request with the permission of the individual. A copy of the declaration of interest form which participants are asked to complete annually is also available on request. A brief outline of the declarations of interest policy is described here and full details of the policy is available on the Clarity Informatics website. Declarations of interests of the authors are not routinely published, however competing interests of all those involved in the topic update or development are listed below. Competing interests include:

  • Personal financial interests
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Although particular attention is given to interests that could result in financial gains or losses for the individual, competing interests may also arise from academic competition or for political, personal, religious, and reputational reasons. An individual is not obliged to seek out knowledge of work done for, or on behalf of, the healthcare industry within the departments for which they are responsible if they would not normally expect to be informed.

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Any individual (or organization) involved in developing, reviewing, or commenting on clinical content, particularly the recommendations should declare competing interests. This includes the authoring team members, expert advisers, external reviewers of draft topics, individuals providing feedback on published topics, and Editorial Steering Group members. Declarations of interest are completed annually for authoring team and editorial steering group members, and are completed at the start of the topic update and development process for external stakeholders.

Competing interests declared for this topic:

None.

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